ClinVar Miner

List of variants in gene BRAF reported as uncertain significance by GeneDx

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Total variants: 57
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HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.977T>C (p.Ile326Thr) rs368435578 0.00003
NM_004333.6(BRAF):c.1165C>T (p.Arg389Cys) rs397507472 0.00002
NM_004333.6(BRAF):c.-9G>T rs1161647286 0.00001
NM_004333.6(BRAF):c.107C>T (p.Ser36Phe) rs886041827 0.00001
NM_004333.6(BRAF):c.1166G>A (p.Arg389His) rs577372072 0.00001
NM_004333.6(BRAF):c.1168G>A (p.Gly390Ser) rs886041424 0.00001
NM_004333.6(BRAF):c.2029G>A (p.Asp677Asn) rs886041260 0.00001
NM_004333.6(BRAF):c.2156G>A (p.Arg719His) rs368528867 0.00001
NM_004333.6(BRAF):c.254A>G (p.Tyr85Cys) rs1131691387 0.00001
NM_004333.6(BRAF):c.365C>A (p.Ser122Tyr) rs397507462 0.00001
NM_004333.6(BRAF):c.41C>G (p.Pro14Arg) rs397507455 0.00001
NM_004333.6(BRAF):c.712G>A (p.Val238Ile) rs373935661 0.00001
NM_004333.6(BRAF):c.112G>T (p.Ala38Ser)
NM_004333.6(BRAF):c.1189G>T (p.Gly397Cys) rs760702929
NM_004333.6(BRAF):c.1207C>G (p.Pro403Ala) rs749792302
NM_004333.6(BRAF):c.1209del (p.Ala404fs)
NM_004333.6(BRAF):c.1258C>T (p.Pro420Ser)
NM_004333.6(BRAF):c.1283C>T (p.Ser428Leu) rs1562957703
NM_004333.6(BRAF):c.1444G>C (p.Val482Leu) rs765715150
NM_004333.6(BRAF):c.159G>A (p.Met53Ile) rs2129073763
NM_004333.6(BRAF):c.1694+2T>C rs1057517930
NM_004333.6(BRAF):c.1726G>T (p.Asp576Tyr) rs1057517915
NM_004333.6(BRAF):c.1750C>T (p.Leu584Phe) rs1586015221
NM_004333.6(BRAF):c.1775T>C (p.Ile592Thr) rs55939351
NM_004333.6(BRAF):c.1807C>T (p.Arg603Ter) rs104886015
NM_004333.6(BRAF):c.1860+3A>G rs886041842
NM_004333.6(BRAF):c.1891A>T (p.Asn631Tyr)
NM_004333.6(BRAF):c.1933G>C (p.Val645Leu)
NM_004333.6(BRAF):c.1940A>G (p.Tyr647Cys) rs1562939198
NM_004333.6(BRAF):c.1976T>C (p.Ile659Thr) rs2128994327
NM_004333.6(BRAF):c.1990C>G (p.Gln664Glu) rs754481830
NM_004333.6(BRAF):c.2026C>T (p.Pro676Ser) rs1554389860
NM_004333.6(BRAF):c.2101A>G (p.Arg701Gly) rs886041257
NM_004333.6(BRAF):c.2134G>A (p.Ala712Thr) rs1481562268
NM_004333.6(BRAF):c.2135C>T (p.Ala712Val) rs727502904
NM_004333.6(BRAF):c.2264_2265delinsGT (p.Ile755Ser) rs1064795542
NM_004333.6(BRAF):c.2291C>T (p.Pro764Leu) rs139420557
NM_004333.6(BRAF):c.260G>A (p.Ser87Asn) rs1033856250
NM_004333.6(BRAF):c.272C>T (p.Ala91Val) rs886041256
NM_004333.6(BRAF):c.27_32dup (p.Gly11_Ala12insGlyGly)
NM_004333.6(BRAF):c.325T>A (p.Phe109Ile) rs397507460
NM_004333.6(BRAF):c.37G>A (p.Glu13Lys) rs1563042573
NM_004333.6(BRAF):c.398C>T (p.Ser133Leu) rs1057517889
NM_004333.6(BRAF):c.48G>C (p.Gln16His) rs1563042542
NM_004333.6(BRAF):c.497G>A (p.Arg166Lys) rs2129061937
NM_004333.6(BRAF):c.517T>C (p.Cys173Arg) rs749677118
NM_004333.6(BRAF):c.69G>T (p.Met23Ile) rs1064796897
NM_004333.6(BRAF):c.70G>A (p.Glu24Lys) rs730880416
NM_004333.6(BRAF):c.73C>A (p.Pro25Thr) rs730880412
NM_004333.6(BRAF):c.812G>A (p.Arg271His) rs730880413
NM_004333.6(BRAF):c.83GCGCCG[1] (p.28GA[1]) rs397507458
NM_004333.6(BRAF):c.83GCGCCG[5] (p.28GA[5]) rs397507458
NM_004333.6(BRAF):c.913G>A (p.Ala305Thr) rs964235659
NM_004333.6(BRAF):c.943G>A (p.Gly315Arg)
NM_004333.6(BRAF):c.956C>T (p.Ser319Phe) rs886041599
NM_004333.6(BRAF):c.967T>C (p.Ser323Pro) rs730880414
NM_004333.6(BRAF):c.973T>G (p.Ser325Ala)

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